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R-N-Cbz-2-Hydroxymethylmorpholine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 500702-97-6 Structure
  • Basic information

    1. Product Name: R-N-Cbz-2-Hydroxymethylmorpholine
    2. Synonyms: R-N-Cbz-2-Hydroxymethylmorpholine;(2R)-2-(Hydroxymethyl)-4-morpholinecarboxylic Acid Phenylmethyl Ester
    3. CAS NO:500702-97-6
    4. Molecular Formula: C13H17NO4
    5. Molecular Weight: 251.27838
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 500702-97-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 413.0±40.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.223±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.36±0.10(Predicted)
    10. CAS DataBase Reference: R-N-Cbz-2-Hydroxymethylmorpholine(CAS DataBase Reference)
    11. NIST Chemistry Reference: R-N-Cbz-2-Hydroxymethylmorpholine(500702-97-6)
    12. EPA Substance Registry System: R-N-Cbz-2-Hydroxymethylmorpholine(500702-97-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 500702-97-6(Hazardous Substances Data)

500702-97-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 500702-97-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,7,0 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 500702-97:
(8*5)+(7*0)+(6*0)+(5*7)+(4*0)+(3*2)+(2*9)+(1*7)=106
106 % 10 = 6
So 500702-97-6 is a valid CAS Registry Number.

500702-97-6Relevant articles and documents

MDM2 DEGRADERS AND USES THEREOF

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Paragraph 001200; 001201-001202, (2021/09/26)

The present invention relates to compounds and methods useful for the modulation of mouse double minute 2 homolog ("MDM2") protein via ubiquitination and/or degradation by compounds according to the present invention.

HETEROCYCLIC SUBSTITUTED UREAS, FOR USE AGAINST CANCER

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Page/Page column 96, (2020/03/02)

The application relates to heterocyclic urea derivatives and their use in the treatment and prophylaxis of cancer, and to compositions containing said derivatives and processes for their preparation.

IRAK DEGRADERS AND USES THEREOF

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Paragraph 00962; 001684-001686, (2020/06/19)

The present invention provides compounds, compositions thereof, and methods of using the same.

IRAK DEGRADERS AND USES THEREOF

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Paragraph 4116; 4117, (2019/07/10)

The present invention provides compounds, compositions thereof, and methods of using the same.

DIHYDROPYRIMIDINE COMPOUNDS AND THEIR APPLICATION IN PHARMACEUTICALS

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Paragraph 00158, (2015/11/24)

Provided herein are dihydropyrimidine compounds and their pharmaceutical applications, especially for use in treating and preventing HBV diseases. Specifically, provided herein are compounds having Formula (I) or (Ia), or an enantiomer, a diastereoisomer,

Disubstituted pyrimidines as Lck inhibitors

Hunt, Julianne A.,Beresis, Richard T.,Goulet, Joung L.,Holmes, Mark A.,Hong, Xinfang J.,Kovacs, Ernest,Mills, Sander G.,Ruzek, Rowena D.,Wong, Frederick,Hermes, Jeffrey D.,Park, Young-Whan,Salowe, Scott P.,Sonatore, Lisa M.,Wu, Lin,Woods, Andrea,Zaller, Dennis M.,Sinclair, Peter J.

supporting information; experimental part, p. 5440 - 5443 (2010/04/26)

We have developed a family of 4-benzimidazolyl-N-piperazinethyl-pyrimidin-2-amines that are subnanomolar inhibitors of Lck. A subset of these Lck inhibitors, with heterocyclic substituents at the benzimidazole C5, are also low-nanomolar inhibitors of cell

Src kinase inhibitor compounds

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, (2008/06/13)

Pyrimidine compounds (Formula I), or their pharmaceutically acceptable salts, hydrates, solvates, crystal forms and individual diastereomers, and pharmaceutical compositions including the same, which are inhibitors of tyrosine kinase enzymes, and as such are useful in the prophylaxis and treatment of protein tyrosine kinase-associated disorders, such as immune diseases, hyperproliferative disorders and other diseases in which inappropriate protein kinase action is believed to play a role, such as cancer, angiogensis, atheroscelerosis, graft rejection, rheumatoid arthritis and psoriasis.

SRC kinase inhibitor compounds

-

, (2008/06/13)

Pyrimidine compounds (Formula I), or their pharmaceutically acceptable salts, hydrates, solvates, crystal forms and individual diastereomers, and pharmaceutical compositions including the same, which are inhibitors of tyrosine kinase enzymes, and as such are useful in the prophylaxis and treatment of protein tyrosine kinase-associated disorders, such as immune diseases, hyperproliferative disorders and other diseases in which inappropriate protein kinase action is believed to play a role, such as cancer, angiogensis, atheroscelerosis, graft rejection, rheumatoid arthritis and psoriasis.

The synthesis of 2-morpholine carboxylic acid derivatives and their elaboration to 1-aza-4-oxabicyclo[3.3.1]nonan-6-one

King,Martin

, p. 2281 - 2284 (2007/10/19)

Two syntheses of novel 2-morpholine carboxylic acid derivatives are described. The esters were converted into 1-aza-4-oxabicyclo[3.3.1]nonan-6-one, the first example of this ring system, which was further elaborated to the ortho-methoxy benzamide derivative (2).

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